Nagy Attila, Wu Jianrong, Berland Keith M
Emory University, Department of Physics, Atlanta, Georgia 30322, USA.
J Biomed Opt. 2005 Jul-Aug;10(4):44015. doi: 10.1117/1.1991860.
Fluorescence correlation spectroscopy (FCS) and related distribution analysis techniques have become extremely important and widely used research tools for analyzing the dynamics, kinetics, interactions, and mobility of biomolecules. However, it is not widely recognized that photophysical dynamics can dramatically influence the calibration of fluctuation spectroscopy instrumentation. While the basic theories for fluctuation spectroscopy methods are well established, there have not been quantitative models to characterize the photophysical-induced variations observed in measured fluctuation spectroscopy data under varied excitation conditions. We introduce quantitative models to characterize how the fluorescence observation volumes in one-photon confocal microscopy are modified by excitation saturation as well as corresponding models for the effect of the volume changes in FCS. We introduce a simple curve fitting procedure to model the role of saturation in FCS measurements and demonstrate its accuracy in fitting measured correlation curves over a wide range of excitation conditions.
荧光相关光谱法(FCS)及相关分布分析技术已成为用于分析生物分子动力学、动力学过程、相互作用及迁移率的极其重要且广泛应用的研究工具。然而,光物理动力学可显著影响波动光谱仪器的校准这一点尚未得到广泛认可。虽然波动光谱方法的基本理论已确立,但尚未有定量模型来表征在不同激发条件下测量的波动光谱数据中观察到的光物理诱导变化。我们引入定量模型来表征单光子共聚焦显微镜中的荧光观察体积如何因激发饱和而改变,以及针对FCS中体积变化影响的相应模型。我们引入一种简单的曲线拟合程序来模拟饱和在FCS测量中的作用,并证明其在广泛激发条件下拟合测量相关曲线的准确性。